ClinVar Miner

Submissions for variant NM_033360.4(KRAS):c.*3672C>G

gnomAD frequency: 0.00016  dbSNP: rs188922523
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000284910 SCV000377635 uncertain significance Noonan syndrome 2016-06-14 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003391094 SCV004134566 benign not provided 2022-07-01 criteria provided, single submitter clinical testing KRAS: BS1, BS2

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